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| Open reading frame (ORF) annotation in the exon skipping event |
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| Splicing Quantitative Trait Loci (sQTLs) in the skipped exons |
| Splicing Quantitative Trait Methylation (sQTM) in the skipped exon |
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Gene summary for CCNB3 |
 Gene summary |
| Gene information | Gene symbol | CCNB3 | Gene ID | 85417 |
| Gene name | cyclin B3 | |
| Synonyms | - | |
| Cytomap | Xp11.22 | |
| Type of gene | protein-coding | |
| Description | G2/mitotic-specific cyclin-B3 | |
| Modification date | 20180523 | |
| UniProtAcc | Q8WWL7 | |
| Context | PubMed: CCNB3 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract] - Title (PMID) |
| Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Gene | GO ID | GO term | PubMed ID |
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Exon skipping events across known transcript of Ensembl for CCNB3 from UCSC genome browser |
| Skipped exons in TCGA and GTEx based on Ensembl gene isoform structure. * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Gene isoform structures and expression levels for CCNB3 |
| Expression levels of gene isoforms across TCGA. |
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| Expression levels of gene isoforms across GTEx. |
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Exon skipping events with PSIs in TCGA for CCNB3 |
| Information of exkip skipping event in TCGA. |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_510552 | X | 50031779:50031887:50037862:50037993:50051504:50054496 | 50037862:50037993 | ENSG00000147082.13 | ENST00000376042.1,ENST00000276014.7 |
| exon_skip_510554 | X | 50037862:50037993:50051504:50054496:50055536:50055632 | 50051504:50054496 | ENSG00000147082.13 | ENST00000376042.1,ENST00000276014.7 |
| exon_skip_510555 | X | 50055536:50055632:50056855:50056948:50085200:50085338 | 50056855:50056948 | ENSG00000147082.13 | ENST00000476167.1,ENST00000376042.1,ENST00000276014.7 |
| PSI values of skipped exons in TCGA. |
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Exon skipping events with PSIs in GTEx for CCNB3 |
| Information of exkip skipping event in GTEx |
| Exon skip ID | chr | Exons involved in exon skipping | Skipped exon | ENSG | ENSTs |
| exon_skip_510552 | X | 50031779:50031887:50037862:50037993:50051504:50054496 | 50037862:50037993 | ENSG00000147082.13 | ENST00000376042.1,ENST00000276014.7 |
| exon_skip_510555 | X | 50055536:50055632:50056855:50056948:50085200:50085338 | 50056855:50056948 | ENSG00000147082.13 | ENST00000376042.1,ENST00000476167.1,ENST00000276014.7 |
| PSI values of skipped exons in GTEx. |
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| * Skipped exon sequences. |
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Open reading frame (ORF) annotation in the exon skipping event for CCNB3 |
| Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms. |
| ENST | Start of skipped exon | End of skipped exon | ORF |
| ENST00000276014 | 50037862 | 50037993 | Frame-shift |
| ENST00000376042 | 50037862 | 50037993 | Frame-shift |
| ENST00000276014 | 50051504 | 50054496 | Frame-shift |
| ENST00000376042 | 50051504 | 50054496 | Frame-shift |
| ENST00000276014 | 50056855 | 50056948 | In-frame |
| ENST00000376042 | 50056855 | 50056948 | In-frame |
| Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms. |
| ENST | Start of skipped exon | End of skipped exon | ORF |
| ENST00000276014 | 50037862 | 50037993 | Frame-shift |
| ENST00000376042 | 50037862 | 50037993 | Frame-shift |
| ENST00000276014 | 50056855 | 50056948 | In-frame |
| ENST00000376042 | 50056855 | 50056948 | In-frame |
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Infer the effects of exon skipping event on protein functional features for CCNB3 |
| Exon skipping at the protein sequence level and followed lost functional features. * Click on the image to enlarge it in a new window. |
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| Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases. |
| ENST | Length of mRNA | Length of AA seq. | Genomic start | Genomic end | mRNA start | mRNA end | AA start | AA end |
| ENST00000276014 | 4526 | 1395 | 50056855 | 50056948 | 3538 | 3630 | 1141 | 1172 |
| ENST00000376042 | 4710 | 1395 | 50056855 | 50056948 | 3722 | 3814 | 1141 | 1172 |
| Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases. |
| ENST | Length of mRNA | Length of AA seq. | Genomic start | Genomic end | mRNA start | mRNA end | AA start | AA end |
| ENST00000276014 | 4526 | 1395 | 50056855 | 50056948 | 3538 | 3630 | 1141 | 1172 |
| ENST00000376042 | 4710 | 1395 | 50056855 | 50056948 | 3722 | 3814 | 1141 | 1172 |
| Lost protein functional features of individual exon skipping events in TCGA. |
| UniProt acc. | Start of exon skipping (AA) | End of exon skipping (AA) | Protein feature start (AA) | Protein feature end (AA) | Category of protein feature | Description of feature |
| Q8WWL7 | 1141 | 1172 | 69 | 1172 | Alternative sequence | ID=VSP_010514;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 69 | 1172 | Alternative sequence | ID=VSP_010514;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 112 | 1395 | Alternative sequence | ID=VSP_010515;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 112 | 1395 | Alternative sequence | ID=VSP_010515;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 1 | 1395 | Chain | ID=PRO_0000080373;Note=G2/mitotic-specific cyclin-B3 |
| Q8WWL7 | 1141 | 1172 | 1 | 1395 | Chain | ID=PRO_0000080373;Note=G2/mitotic-specific cyclin-B3 |
| Lost protein functional features of individual exon skipping events in GTEx. |
| UniProt acc. | Start of exon skipping (AA) | End of exon skipping (AA) | Protein feature start (AA) | Protein feature end (AA) | Category of protein feature | Description of feature |
| Q8WWL7 | 1141 | 1172 | 69 | 1172 | Alternative sequence | ID=VSP_010514;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 69 | 1172 | Alternative sequence | ID=VSP_010514;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 112 | 1395 | Alternative sequence | ID=VSP_010515;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 112 | 1395 | Alternative sequence | ID=VSP_010515;Note=In isoform 3. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:11846420;Dbxref=PMID:11846420 |
| Q8WWL7 | 1141 | 1172 | 1 | 1395 | Chain | ID=PRO_0000080373;Note=G2/mitotic-specific cyclin-B3 |
| Q8WWL7 | 1141 | 1172 | 1 | 1395 | Chain | ID=PRO_0000080373;Note=G2/mitotic-specific cyclin-B3 |
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SNVs in the skipped exons for CCNB3 |
| - Lollipop plot for presenting exon skipping associated SNVs. * Click on the image to enlarge it in a new window. |
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| - Differential PSIs between mutated versus non-mutated samples. |
| - Non-synonymous mutations located in the skipped exons in TCGA. |
| Cancer type | Sample | ESID | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| BRCA | TCGA-AR-A1AI-01 | exon_skip_510554 | 50051505 | 50054496 | 50052008 | 50052008 | Frame_Shift_Del | C | - | p.H281fs |
| ESCA | TCGA-L5-A8NM-01 | exon_skip_510554 | 50051505 | 50054496 | 50052616 | 50052616 | Frame_Shift_Del | C | - | p.T485fs |
| LIHC | TCGA-DD-A1EG-01 | exon_skip_510554 | 50051505 | 50054496 | 50053617 | 50053617 | Frame_Shift_Del | C | - | p.L816fs |
| LIHC | TCGA-DD-A39Y-01 | exon_skip_510554 | 50051505 | 50054496 | 50053624 | 50053624 | Frame_Shift_Del | C | - | p.P819fs |
| ACC | TCGA-OR-A5KB-01 | exon_skip_510554 | 50051505 | 50054496 | 50054083 | 50054083 | Frame_Shift_Del | G | - | p.G972fs |
| ACC | TCGA-OR-A5KB-01 | exon_skip_510554 | 50051505 | 50054496 | 50054083 | 50054083 | Frame_Shift_Del | G | - | p.V971fs |
| LUAD | TCGA-95-7567-01 | exon_skip_510554 | 50051505 | 50054496 | 50051702 | 50051703 | Frame_Shift_Ins | - | A | p.*178fs |
| LUAD | TCGA-95-7567-01 | exon_skip_510554 | 50051505 | 50054496 | 50051702 | 50051703 | Frame_Shift_Ins | - | A | p.L178fs |
| LIHC | TCGA-BC-A112-01 | exon_skip_510554 | 50051505 | 50054496 | 50052937 | 50052938 | Frame_Shift_Ins | - | A | p.K590fs |
| UCEC | TCGA-BS-A0UF-01 | exon_skip_510554 | 50051505 | 50054496 | 50051794 | 50051794 | Nonsense_Mutation | G | T | p.E209* |
| UCEC | TCGA-B5-A0JY-01 | exon_skip_510554 | 50051505 | 50054496 | 50051905 | 50051905 | Nonsense_Mutation | G | T | p.E246* |
| SKCM | TCGA-DA-A95Z-06 | exon_skip_510554 | 50051505 | 50054496 | 50052151 | 50052151 | Nonsense_Mutation | C | T | p.Q328* |
| UCEC | TCGA-BS-A0TC-01 | exon_skip_510554 | 50051505 | 50054496 | 50052167 | 50052167 | Nonsense_Mutation | T | A | p.L333* |
| UCEC | TCGA-BS-A0UV-01 | exon_skip_510554 | 50051505 | 50054496 | 50052215 | 50052215 | Nonsense_Mutation | C | A | p.S349* |
| UCEC | TCGA-AP-A0LM-01 | exon_skip_510554 | 50051505 | 50054496 | 50052433 | 50052433 | Nonsense_Mutation | G | T | p.E422* |
| UCEC | TCGA-BS-A0UF-01 | exon_skip_510554 | 50051505 | 50054496 | 50052433 | 50052433 | Nonsense_Mutation | G | T | p.E422* |
| LUAD | TCGA-55-A494-01 | exon_skip_510554 | 50051505 | 50054496 | 50052923 | 50052923 | Nonsense_Mutation | C | A | p.S585* |
| LUAD | TCGA-86-8073-01 | exon_skip_510554 | 50051505 | 50054496 | 50053081 | 50053081 | Nonsense_Mutation | G | T | p.E638* |
| UCEC | TCGA-AX-A05Z-01 | exon_skip_510554 | 50051505 | 50054496 | 50053138 | 50053138 | Nonsense_Mutation | G | T | p.E657* |
| UCEC | TCGA-BS-A0UV-01 | exon_skip_510554 | 50051505 | 50054496 | 50053291 | 50053291 | Nonsense_Mutation | A | T | p.K708* |
| UCEC | TCGA-B5-A0JY-01 | exon_skip_510554 | 50051505 | 50054496 | 50053330 | 50053330 | Nonsense_Mutation | G | T | p.E721* |
| THYM | TCGA-XU-A92Y-01 | exon_skip_510554 | 50051505 | 50054496 | 50053477 | 50053477 | Nonsense_Mutation | G | T | p.E770X |
| UCEC | TCGA-A5-A0GP-01 | exon_skip_510554 | 50051505 | 50054496 | 50054374 | 50054374 | Nonsense_Mutation | G | T | p.E1069* |
| - Depth of coverage in the three exons composing exon skipping event |
| Depth of coverage in three exons | Mutation description |
| - Non-synonymous mutations located in the skipped exons in CCLE. |
| Sample | Skipped exon start | Skipped exon end | Mutation start | Mutation end | Mutation type | Reference seq | Mutation seq | AAchange |
| A498_KIDNEY | 50037863 | 50037993 | 50037945 | 50037946 | Frame_Shift_Del | AC | - | p.N96fs |
| SNU761_LIVER | 50051505 | 50054496 | 50051869 | 50051869 | Frame_Shift_Del | A | - | p.K234fs |
| JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50052616 | 50052616 | Frame_Shift_Del | C | - | p.P484fs |
| CW2_LARGE_INTESTINE | 50051505 | 50054496 | 50052663 | 50052663 | Frame_Shift_Del | G | - | p.Q498fs |
| UMUC5_URINARY_TRACT | 50037863 | 50037993 | 50037973 | 50037973 | Missense_Mutation | G | C | p.K105N |
| SNU81_LARGE_INTESTINE | 50051505 | 50054496 | 50051565 | 50051565 | Missense_Mutation | G | T | p.E132D |
| MCC13_SKIN | 50051505 | 50054496 | 50051626 | 50051626 | Missense_Mutation | C | T | p.L153F |
| CROAP3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50051689 | 50051689 | Missense_Mutation | A | G | p.K174E |
| HCC2998_LARGE_INTESTINE | 50051505 | 50054496 | 50051690 | 50051690 | Missense_Mutation | A | C | p.K174T |
| AN3CA_ENDOMETRIUM | 50051505 | 50054496 | 50051696 | 50051696 | Missense_Mutation | T | C | p.L176S |
| ESS1_ENDOMETRIUM | 50051505 | 50054496 | 50051719 | 50051719 | Missense_Mutation | C | A | p.H184N |
| KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50051743 | 50051743 | Missense_Mutation | A | G | p.K192E |
| SCC3_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50051743 | 50051743 | Missense_Mutation | A | G | p.K192E |
| CW2_LARGE_INTESTINE | 50051505 | 50054496 | 50051925 | 50051925 | Missense_Mutation | G | T | p.Q252H |
| JHUEM7_ENDOMETRIUM | 50051505 | 50054496 | 50051976 | 50051976 | Missense_Mutation | G | T | p.K269N |
| RKO_LARGE_INTESTINE | 50051505 | 50054496 | 50051989 | 50051989 | Missense_Mutation | A | C | p.T274P |
| HEC251_ENDOMETRIUM | 50051505 | 50054496 | 50052023 | 50052023 | Missense_Mutation | C | A | p.S285Y |
| HUPT4_PANCREAS | 50051505 | 50054496 | 50052043 | 50052043 | Missense_Mutation | A | G | p.I292V |
| KARPAS422_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50052053 | 50052053 | Missense_Mutation | A | C | p.K295T |
| HUH28_BILIARY_TRACT | 50051505 | 50054496 | 50052128 | 50052128 | Missense_Mutation | C | T | p.T320I |
| PL21_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50052141 | 50052141 | Missense_Mutation | G | T | p.E324D |
| EN_ENDOMETRIUM | 50051505 | 50054496 | 50052188 | 50052188 | Missense_Mutation | A | G | p.E340G |
| MIAPACA2_PANCREAS | 50051505 | 50054496 | 50052208 | 50052208 | Missense_Mutation | A | G | p.K347E |
| MCC13_SKIN | 50051505 | 50054496 | 50052253 | 50052253 | Missense_Mutation | C | T | p.L362F |
| LU139_LUNG | 50051505 | 50054496 | 50052357 | 50052358 | Missense_Mutation | CC | TT | p.R397C |
| LNCAPCLONEFGC_PROSTATE | 50051505 | 50054496 | 50052373 | 50052373 | Missense_Mutation | G | T | p.V402L |
| FARAGE_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50052437 | 50052437 | Missense_Mutation | A | C | p.K423T |
| SNU1040_LARGE_INTESTINE | 50051505 | 50054496 | 50052506 | 50052506 | Missense_Mutation | A | G | p.E446G |
| NCIH2171_LUNG | 50051505 | 50054496 | 50052530 | 50052530 | Missense_Mutation | C | A | p.P454H |
| KMH2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50052631 | 50052631 | Missense_Mutation | C | G | p.P488A |
| HEC251_ENDOMETRIUM | 50051505 | 50054496 | 50052694 | 50052694 | Missense_Mutation | A | G | p.I509V |
| HEC59_ENDOMETRIUM | 50051505 | 50054496 | 50052707 | 50052707 | Missense_Mutation | C | T | p.T513I |
| JHUEM7_ENDOMETRIUM | 50051505 | 50054496 | 50052892 | 50052892 | Missense_Mutation | A | C | p.T575P |
| MERO48A_LUNG | 50051505 | 50054496 | 50052903 | 50052903 | Missense_Mutation | G | T | p.E578D |
| HEC251_ENDOMETRIUM | 50051505 | 50054496 | 50052916 | 50052916 | Missense_Mutation | A | G | p.K583E |
| NCIH1836_LUNG | 50051505 | 50054496 | 50052955 | 50052955 | Missense_Mutation | G | T | p.G596W |
| RPMI8866_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50053010 | 50053010 | Missense_Mutation | A | G | p.E614G |
| JHUEM7_ENDOMETRIUM | 50051505 | 50054496 | 50053020 | 50053020 | Missense_Mutation | C | A | p.F617L |
| NCIH1915_LUNG | 50051505 | 50054496 | 50053035 | 50053035 | Missense_Mutation | G | T | p.L622F |
| CCFSTTG1_CENTRAL_NERVOUS_SYSTEM | 50051505 | 50054496 | 50053064 | 50053064 | Missense_Mutation | A | G | p.E632G |
| EFM192A_BREAST | 50051505 | 50054496 | 50053066 | 50053066 | Missense_Mutation | A | G | p.K633E |
| HGC27_STOMACH | 50051505 | 50054496 | 50053127 | 50053127 | Missense_Mutation | C | T | p.S653F |
| HGC27_STOMACH | 50051505 | 50054496 | 50053127 | 50053128 | Missense_Mutation | CC | TT | p.S653F |
| RKO_LARGE_INTESTINE | 50051505 | 50054496 | 50053151 | 50053151 | Missense_Mutation | T | C | p.I661T |
| FUOV1_OVARY | 50051505 | 50054496 | 50053276 | 50053276 | Missense_Mutation | G | A | p.E703K |
| ESS1_ENDOMETRIUM | 50051505 | 50054496 | 50053419 | 50053419 | Missense_Mutation | G | T | p.K750N |
| MEWO_SKIN | 50051505 | 50054496 | 50053439 | 50053439 | Missense_Mutation | G | A | p.G757E |
| LN18_CENTRAL_NERVOUS_SYSTEM | 50051505 | 50054496 | 50053463 | 50053463 | Missense_Mutation | A | C | p.Q765P |
| SISO_CERVIX | 50051505 | 50054496 | 50053630 | 50053630 | Missense_Mutation | A | G | p.I821V |
| GRST_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50053630 | 50053630 | Missense_Mutation | A | G | p.I821V |
| OVCAR4_OVARY | 50051505 | 50054496 | 50053651 | 50053651 | Missense_Mutation | A | G | p.K828E |
| NCIH1435_LUNG | 50051505 | 50054496 | 50053740 | 50053740 | Missense_Mutation | G | T | p.K857N |
| JHUEM7_ENDOMETRIUM | 50051505 | 50054496 | 50053782 | 50053782 | Missense_Mutation | G | T | p.E871D |
| NCIBL2126_MATCHED_NORMAL_TISSUE | 50051505 | 50054496 | 50053810 | 50053810 | Missense_Mutation | T | C | p.W881R |
| NCIH2126_LUNG | 50051505 | 50054496 | 50053810 | 50053810 | Missense_Mutation | T | C | p.W881R |
| MDAMB361_BREAST | 50051505 | 50054496 | 50053817 | 50053817 | Missense_Mutation | A | T | p.K883M |
| SW982_SOFT_TISSUE | 50051505 | 50054496 | 50053818 | 50053818 | Missense_Mutation | G | T | p.K883N |
| MEWO_SKIN | 50051505 | 50054496 | 50054071 | 50054071 | Missense_Mutation | G | T | p.V968F |
| KYSE140_OESOPHAGUS | 50051505 | 50054496 | 50054113 | 50054113 | Missense_Mutation | C | T | p.P982S |
| MESSA_SOFT_TISSUE | 50051505 | 50054496 | 50054263 | 50054263 | Missense_Mutation | G | A | p.A1032T |
| HCC366_LUNG | 50051505 | 50054496 | 50054336 | 50054336 | Missense_Mutation | G | A | p.S1056N |
| HT115_LARGE_INTESTINE | 50051505 | 50054496 | 50054376 | 50054376 | Missense_Mutation | G | T | p.E1069D |
| NCIH3255_LUNG | 50051505 | 50054496 | 50054381 | 50054381 | Missense_Mutation | C | A | p.S1071Y |
| BE13_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50054381 | 50054381 | Missense_Mutation | C | T | p.S1071F |
| HCT15_LARGE_INTESTINE | 50056856 | 50056948 | 50056863 | 50056863 | Missense_Mutation | T | C | p.F1144S |
| YT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50056856 | 50056948 | 50056904 | 50056904 | Missense_Mutation | A | T | p.S1158C |
| KMBC2_URINARY_TRACT | 50056856 | 50056948 | 50056912 | 50056912 | Missense_Mutation | G | A | p.M1160I |
| HS445_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE | 50051505 | 50054496 | 50051941 | 50051941 | Nonsense_Mutation | G | T | p.E258* |
| SW403_LARGE_INTESTINE | 50051505 | 50054496 | 50052433 | 50052433 | Nonsense_Mutation | G | T | p.E422* |
| LB647SCLC_LUNG | 50051505 | 50054496 | 50053779 | 50053780 | Nonsense_Mutation | GG | AT | p.E871* |
| DOK_UPPER_AERODIGESTIVE_TRACT | 50051505 | 50054496 | 50053795 | 50053795 | Nonsense_Mutation | C | T | p.R876* |
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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for CCNB3 |
| sQTL information located at the skipped exons. |
| Exon skip ID | Chromosome | Three exons | Skippped exon | ENST | Cancer type | SNP id | Location | DNA change (ref/var) | P-value |
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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for CCNB3 |
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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for CCNB3 |
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RelatedDrugs for CCNB3 |
| Approved drugs targeting this gene. (DrugBank Version 5.1.0 2018-04-02) |
| Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for CCNB3 |
| Diseases associated with this gene. (DisGeNet 4.0) |
| Gene | Disease ID | Disease name | # pubmeds | Source |
| CCNB3 | C0029463 | Osteosarcoma | 1 | CTD_human |
Copyright 2018-Present -The University of Texas Health Science Center at Houston (UTHealth)
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